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VenenWalker Pro2

EUDAMED

Class IIa (EU MDR)

Ref 001-1011-00

by Zero-Plus International Limited

Identity

Trade Name
VenenWalker PRO2 EUDAMED
Device Name
VenenWalker Pro2 EUDAMED
Model / Reference
001-1011-00 EUDAMED

Identifiers

Primary DI / UDI-DI
04897112840022 EUDAMED
D-VWP2-GMBB EUDAMED
Basic UDI-DI
B-04897112840022 EUDAMED
B-VWP2-GMBB EUDAMED
EMDN Code
Z120607 PNEUMATIC COMPRESSION EQUIPMENT EUDAMED

Classification

Device Class
Class IIa EUDAMED
Market of Registration
Germany EUDAMED

Clinical & Handling

Sterile

No

EUDAMED

Implantable

No

EUDAMED

Reusable

No

EUDAMED

Contains Latex

No

EUDAMED

Reprocessed

No

EUDAMED

Human-derived

No

EUDAMED

Human Tissues

No

EUDAMED

Animal Tissues

No

EUDAMED

Administering Medicine

No

EUDAMED

Measuring Function

No

EUDAMED

Incorporates Medicinal Product

No

EUDAMED

VenenWalker Pro2 by Zero-Plus International Limited — Class IIa — MDD — listed in EUDAMED — regulatory data on deviCERTS

Authorization Coverage (European Union — 27 member states)

Regulatory Authorizations

European Union Active

CE/MDD

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Manufacturer

EUDAMED SRN
HK-MF-000018103
Authorised Representative
Globalmind consumer electronics GmbH DE-AR-000014256

Sources (2)

  • EUDAMED 14d56ded-e2d2-4e7e-aa34-f49c9c98e3f2 61 fields · synced Jul 9, 2026
  • EUDAMED 76c48b71-7e81-45a2-8185-529a8cd45620 61 fields · synced May 17, 2026